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A K Schmid

Publications and source records attributed to A K Schmid.

10 recordsLinked to original sources

Spin-dependent quantum interference from epitaxial MgO thin films on Fe(001).

Spin-dependent electron reflection from MgO thin films grown on Fe(001) was measured using spin-polarized low energy electron microscopy. The electron reflectivity exhibits quantum interference from which two MgO energy bands with Delta1 symmetry were determined in experiment. We found that a bulklike MgO energy gap is fully established for MgO film thicker than 3 atomic monolayers and that the electron reflectivity from the MgO/Fe interface exhibits a spin-dependent amplitude and a spin-independent phase change.

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Self-assembled nanofold network formation on layered crystal surfaces during metal intercalation.

We study the formation of planar network nanostructures, which develop during metal deposition on initially smooth surfaces of layered compounds. Using in situ low-energy electron microscopy for dynamic observation and high-resolution transmission electron microscopy for structure analysis, we have observed the rapid formation of hexagonal networks of linear "nanofolds" with prismatic cavities on top of layered VSe2 crystals. Their formation results from relaxation of compressive strains which build up during Cu intercalation into a thin surface layer.

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Spin-induced forbidden evanescent states in III-V semiconductors.

Within the band gap of a semiconductor no electronic propagating states are allowed, but there exist evanescent states which govern charge transport such as tunneling. In this Letter, we address the issue of their spin dependence in III-V semiconductors. Taking into account the spin-orbit interaction, we treat the problem using a k . p 14 x 14 Hamiltonian that we numerically compute for GaAs. Our results show that the removed spin degeneracy in the band gap can lead to giant energy splittings and induces forbidden zones in space where evanescent states are suppressed.

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Magnetic bistability of Co nanodots.

Size-dependent magnetic single-domain versus vortex state stability of Co/Ru(0001) nanodots is explored with spin-polarized low-energy electron microscopy, analytical modeling, and micromagnetic simulations. We show that both single-domain and vortex states can be stabilized in a broad region near the phase boundary. The calculated width of the bistability region and temperature dependent heights of the energy barriers between both states agree well with our experimental findings.

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Spin-dependent Fabry-Pérot interference from a Cu thin film grown on fcc Co(001).

Spin-dependent electron reflection from a Cu thin film grown on Co/Cu(001) was investigated using spin-polarized low-energy electron microscopy (SPLEEM). Fabry-Pe rot type interference was observed and is explained using the phase accumulation model. SPLEEM images of the Cu overlayer reveal magnetic domains in the Co underlayer, with the domain contrast oscillating with electron energy and Cu film thickness. This behavior is attributed to the spin-dependent electron reflectivity at the Cu/Co interface which leads to spin-dependent Fabry-Pe rot electron interference in the Cu film.

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Strain relief through heterophase interface reconstruction: Ag(111)/Ru(0001).

We report an experimental (scanning tunneling microscopy) and theoretical (embedded atom method) study of a heterophase interface reconstruction between Ag(111) and Ru(0001). Despite the large 7% mismatch, the second layer of Ag from the Ru exhibits a hexagonal structure with Ag bulk spacing, providing a close match to bulk Ag. The first layer of Ag (next to Ru) is reconstructed in a highly symmetrical and regular structure containing monolayer long threading dislocations. We argue that this structure may generally occur to relieve strain in a certain class of heterophase interfaces.

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Linking surface stress to surface structure: measurement of atomic strain in a surface alloy using scanning tunneling microscopy.

Annealed submonolayer CoAg/Ru(0001) films form an alloy with a structure that contains droplets of Ag surrounded by Co [G. E. Thayer, V. Ozolins, A. K. Schmid, N. C. Bartelt, M. Asta, J. J. Hoyt, S. Chiang, and R. Q. Hwang, Phys. Rev. Lett. 86, 660 (2001)]. To understand how surface stress contributes to the formation of this structure, we use scanning tunneling microscopy to extract atomic displacements at the boundaries between regions of Co and Ag. Comparing our measurements to Frenkel-Kontorova model calculations, we show how stress due to lattice mismatch contributes to the formation of the alloy droplet structure. In particular, we quantitatively evaluate how competing strain and chemical energy contributions determine surface structure.

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Direct observation of misfit dislocation glide on surfaces.

Using scanning tunneling microscopy we have observed thermally induced dislocation glide in monolayer Cu films on Ru(0001) at room temperature. The motion is governed by a Peierls barrier that depends on the detailed structure of the dislocations, in particular upon whether the threading dislocations that terminate them are dissociated or not. Calculations based on the Frenkel-Kontorova model reproduce the threading dislocation structure and provide estimates of the Peierls barrier and dislocation stiffness which are consistent with experiment.

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Role of stress in thin film alloy thermodynamics: competition between alloying and dislocation formation.

Using scanning tunneling microscopy (STM) and first-principles local-spin-density-approximation calculations to study submonolayer films of Co (1-c)Ag (c)/Ru(0001) alloys, we have discovered a novel phase-separation mechanism. When the Ag concentration c exceeds 0.4, the surface phase separates between a dislocated, pure Ag phase and a pseudomorphically strained Co(0.6)Ag (0.4) surface alloy. We attribute the phase separation to the competition between two stress relief mechanisms: surface alloying and dislocation formation. The agreement between STM measurements and our calculated phase diagram supports this interpretation.

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Alloying at surfaces by the migration of reactive two-dimensional islands.

We have studied the formation kinetics of the copper-tin alloy bronze when tin is deposited on the (111) surface of copper at room temperature. Low-energy electron microscopy and atomic-resolution scanning tunneling microscopy reveal that bronze forms on the surface by a complicated, unanticipated cooperative mechanism: Ordered two-dimensional tin islands containing several hundred thousand atoms spontaneously sweep across the surface, leaving bronze alloys in their tracks. We propose that this process, driven by surface free energy, is a version of the "camphor dance" observed on liquid surfaces, and should be a general mechanism of surface alloying when surface diffusion is faster than exchange into the substrate.

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